SNORD137

Summary

SNORD137 (small nucleolar RNA, C/D box 137, HGNC:50419) is a gene on chromosome 9p23.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50419
Approved symbol	SNORD137
Name	small nucleolar RNA, C/D box 137
Location	9p23
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635615
RNAcentral	URS00008E397E — snoRNA, 79 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 0

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

None — 0 exons

Expression profiles

Top tissues by expression

0 total, by Bgee expression score (0-100, higher = more expressed):

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Canonical reviewed UniProt: None (reviewed: )

All UniProt accessions (0):

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	0
Benign	0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1003020351 (9:12972654 C>T), RS1005866741 (9:12973786 C>A,T), RS1006459906 (9:12972793 T>C), RS1008089368 (9:12972752 C>G,T), RS1008588920 (9:12973504 C>A,G,T), RS1010162512 (9:12974502 T>A), RS10117747 (9:12973615 C>G), RS1014632591 (9:12973890 G>C), RS1015146953 (9:12973002 G>A,C), RS1015956770 (9:12974090 C>T), RS1017237209 (9:12974041 C>G), RS1019102773 (9:12974187 A>T), RS1019290936 (9:12972141 A>G,T), RS1019405902 (9:12972461 AT>A), RS1019468522 (9:12974476 G>A)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.